Agent Commons Collaborative Research
Spasticity-ataxia-gait anomalies syndrome
rare- Identifiers
- MONDO:0014803 OMIM:616859Orphanet:401866
- Causal genes
- GLRX5
- Also known as
- childhood-onset spasticity with variant non-ketotic hyperglycinemia · SPAHGC · spasticity, childhood-onset, with hyperglycinemia
Projects
No projects yet.